UGT1A1 Gene Hyperbilirubinemia Familial Transient Neonatal NGS Genetic DNA Test
Introduction
The UGT1A1 Gene Hyperbilirubinemia Familial Transient Neonatal NGS Genetic DNA Test is a revolutionary diagnostic tool designed to identify genetic predispositions to hyperbilirubinemia in newborns. Hyperbilirubinemia, characterized by elevated levels of bilirubin in the blood, often leads to jaundice in infants. This test employs Next-Generation Sequencing (NGS) technology to accurately detect mutations in the UGT1A1 gene, which is critical for bilirubin metabolism.
What the Test Measures
This genetic test specifically measures the presence of mutations in the UGT1A1 gene. By identifying these mutations, healthcare providers can assess the risk of developing neonatal jaundice and plan appropriate interventions.
Who Should Consider This Test?
Parents or caregivers should consider the UGT1A1 Gene Hyperbilirubinemia test if:
- The newborn exhibits symptoms of jaundice, such as yellowing of the skin or eyes.
- There is a family history of hyperbilirubinemia or related genetic disorders.
- Parents wish to understand the genetic risks associated with bilirubin metabolism.
Benefits of Taking the Test
- Early identification of genetic predispositions can lead to timely interventions.
- Informs healthcare providers for better management of jaundice in newborns.
- Provides peace of mind for parents regarding their child’s health.
Understanding Your Results
Results from the UGT1A1 Gene Hyperbilirubinemia test will indicate whether any mutations were detected in the UGT1A1 gene. A genetic counselor or healthcare provider will guide you through the implications of the results, helping you understand any necessary follow-up actions.
Test Pricing
| Discount Price | 400,000 NGN |
|---|---|
| Regular Price | 560,000 NGN |
Booking Information
To book the UGT1A1 Gene Hyperbilirubinemia Familial Transient Neonatal NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions and guide you through the booking process.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient who is going for UGT1A1 Gene Hyperbilirubinemia, familial transient neonatal NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UGT1A1 Gene Hyperbilirubinemia.
Ensure your newborn’s health by understanding their genetic risks. Book the UGT1A1 Gene Hyperbilirubinemia test today!
